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Personalized Spine Study Group (PSSG) Registry

NCT04601363 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 1000

Last updated 2024-10-03

No results posted yet for this study

Summary

The primary objective of the study is a data collection initiative. The study will collect clinical and radiographic outcomes of patients implanted with patient specific rods. The secondary objective is to collect clinical and radiographic outcomes of patients with hardware as a control cohort to the patient-specific rods.

Conditions

  • Scoliosis; Adolescence
  • Degenerative Disc Disease
  • Spinal Fusion
  • Kyphoscoliosis
  • Pseudoarthrosis of Spine
  • Spinal Stenosis
  • Kyphoses, Scheuermann

Interventions

DEVICE

Patient Specific Rod

Posterior spinal fusion rod

Sponsors & Collaborators

  • Personalized Spine Study Group

    collaborator UNKNOWN

  • University of Colorado, Denver

    lead OTHER

Eligibility

Min Age
10 Years
Max Age
85 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-10-29
Primary Completion
2030-04-30
Completion
2030-04-30

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04601363 on ClinicalTrials.gov